Prof. Shantanu Pal
Dean – Under Graduate Programs
Professor
- Room no 206, SBS
- 0674 7135148
- spal@iitbbs.ac.in
- School of Basic Sciences
Publications
Research Group
Projects
Courses Taught
Experience
Conferences
Publications
- A. Panda, R. G. Biswas, S. Pal “A unified and common intermediate strategy for the asymmetric total synthesis of 3-deoxy-neo-inositol and conduritol E” Tetrahedron Lett. 2016, 57, 36253628.
- A. Panda, S. Satpati, A. Dixit and S. Pal “Novel homologated-apio adenosine derivatives as A3 adenosine receptor agonists: design, synthesis and molecular docking studies” RSC Adv., 2016, 6, 11233-11239.
- A. Panda, S. Islam, M. K. Santra and S. Pal Lead tetraacetate mediated one pot oxidative cleavage and acetylation reaction: An approach to apio and homologated apio pyrimidine nucleosides and their anticancer activity RSC Adv., 2015, 5, 82450-82459.
- S. Das, A. Panda and S. Pal A common and versatile synthetic route to (−) and (+) pentenomycin I, (+) halopentenomycin I and dehydropentenomycin Carbohydr. Res., 2015, 416, 2431.
- A. Panda, S. Das and S. Pal Highly regio- and diastereoselective, acidic clay supported intramolecular nitrile oxidealkene cycloaddition on D-ribose derived nitriles: an efficient synthetic route to isoxazoline fused five and six membered carbocycles. Carbohydr. Res., 2014, 398, 1318.
- S. Pal, W. J. Cho, S. A. Choe, C. Heller, Z. G. Gao, M. Chinn, K. A. acobson, X. Hou, S. K. Lee, H. O. Kim, L. S. Jeong Structureactivity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists Bioorg. Med. Chem. 2009, 17, 3733-3738.
- L. S. Jeong, S. Pal, S. A. Choe, W. J. Choi, K. A. Jacobson, Z. G. Gao, A. M. Klutz, X. Hou, H.O. Kim, H. W. Lee, S. K. Lee, D. K. Tosh, H. R. Moon Structureactivity relationships of truncated D and L-4-thioadenosine derivatives as highly potent and selective as human A3 adenosine receptor antagonists J. Med. Chem. 2008, 51, 6609-6613.
- X. Hou, S. Pal, W. J. Choi, H. O. Kim, A. Tipnis, K. A. Jacobson and L. S. Jeong. Design and synthesis of truncated 4-thioadenosine derivatives as potent and selective A3 adenosine receptor Nucleic Acids Symposium Series 2008, 52, 641-642.
- D. K. Tosh, W. J. Choi, H. O. Kim, Y. Lee, S. Pal, X. Hou, J. Choi, S. Choi, L. S. Jeong Stereoselective synthesis and conformational study of novel 2,3-Didehydro-2,3-dideoxy-4-selenonucleoside. J. Org. Chem. 2008, 73, 4259-4262.
- L. S. Jeong, H. W. Lee, H. O. Kim, D. K. Tosh, S. Pal; W. J. Choi, Z. G. Gao, A. R. Patel, W. Williams, K. A. Jacobson, H. D. Kim Structureactivity relationships of 2-Chloro-N6-substituted-4-thioadenosine-5-N,N-dialkyluronamides as human A3 adenosine receptor antagonists Biorg. Med. Chem. Lett. 2008, 18, 1612-1616.
- L. S. Jeong, L. X. Zhao, W. J. Choi, S. Pal, Y. H. Park, S. K. Lee, M. W. Chum, Y. B. Lee, C. H. Anh, H. R. Moon Synthesis and Antitumor activity of fluorocyclopentenyl-pyrimidines. Nucleosides, Nucleotides Nucleic acids 2007, 26, 713-716.
- M. W. Chum, H. W. Lee, J. H. Kim, H. O. Kim, K. Man, S. Pal; H. R. Moon, L. S. Jeong Stereoselective synthesis of Homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase Nucleosides, Nucleotides Nucleic acids, 2007, 26, 729-732.
- T. Wang, H. J. Lee, D. K. Tosh, H. O. Kim, S. Pal, S. Choi, Y. Lee, H. R. Moon, L. X. Zhao, K. M. Lee, L. S. Jeong Design, synthesis, and molecular modeling studies of 5-deoxy-5-ureidoadenosine: 5-ureido group as multiple hydrogen bonding donors in the active site of S-adenosylhomocysteine hydrolase. Biorg. Med. Chem. Lett., 2007, 17, 4456-4459.
- V. Singh, S. Pal, D. K Tosh, S. M. Mobin Molecular complexity from aromatics, cycloaddition of cyclohexa-2,4-dienones, sigmatropic 1,2-acyl shift and ring-closing metathesis: A new, efficient, and stereoselective synthesis of (±) hirsutic acid C and medium ring carbocycles Tetrahedron, 2007, 63, 2446-2454.
- V. Singh, S. Pal, S. M. Mobin Cycloaddition between electron deficient -systems, photochemical and radical induced reactions: A novel, general and stereoselective route to polyfunctionalised bridge bicyclo[2.2.2]octanes, bicyclo[3.3.0]-, [4.2.0]octanes and tricycle[4.3.1.03,7]decanes. J. Org. Chem., 2006, 71, 3014-3025.
- V. Singh, S. Lahiri, S. Pal. Molecular complexity from aromatics: Synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane: A stereoselective route to tricyclic framework of protoilludanes Biorg. Med. Chem. Lett., 2005, 15, 4367-4369.
- V. Singh, S. Pal, S. M. Mobin Cycloaddition of cyclohexa-2,4-dienones with electron deficient 2 partners: A novel and stereoselective route to functionlised bicyclo[2.2.2]octenones. Chem. Commum., 2002, 2050-2051.
Book Chapters
1. L. S. Jeong, D. K. Tosh, S. Pal “Synthesis of fluoroneplanocin A” In Current protocols in nucleic acid chemistry ed. Beaucage, S. L. John Wiley & Sons: New York 2008, Chapter 14, unit 14.6.
2. D. K. Tosh, H. O. Kim, S. Pal, J. A. Lee and L. S. Jeong “Synthesis and biological activity of Neplanocin A and analogues” In Modified Nucleosides: in biochemistry, biotechnology and medicine ed. Herdewijn, P. John Wiley & Sons: New York 2008, Chapter 21, pp 525.
Review
V. Singh, S. I. Iyer, S. Pal “Recent approaches towards synthesis of cis-decalins” Tetrahedron 2005, 61, 9197-9231.
Research Group
Ph. D. : 2 (completed) 3 (continuing). M. Sc. : 2 (continuing); 13 (completed)
Projects
Courses Taught
- Concept of Organic Synthesis (CY5L003),
- Advaned Organic Chemistry (CY5L007),
- Advanced Heterocyclic Chemistry (CY7L031),
- Organic Chemistry Laboratory (CY5P001),
- Chemistry Laboratory(CY1P001),
- Preparatory Chemistry.
Experience
Conferences